170 results on '"Cummings, Shelly"'
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2. Cancer Risk Associated With PTEN Pathogenic Variants Identified Using Multigene Hereditary Cancer Panel Testing
3. Multigene assessment of genetic risk for women for two or more breast cancers
4. Age of ovarian cancer diagnosis among BRIP1, RAD51C, and RAD51D mutation carriers identified through multi-gene panel testing
5. Prospective Statewide Study of Universal Screening for Hereditary Colorectal Cancer: The Ohio Colorectal Cancer Prevention Initiative
6. Pan-Cancer Panel Testing: Variation in Testing and Results by Ancestry [27O]
7. Abstract P5-03-03: Variant Classification Discordance: A real-world experience of genetic test results in a community-based setting
8. Association of Genomic Instability Score, Tumor Mutational Burden, and Tumor-Infiltrating Lymphocytes as Biomarkers in Uterine Serous Carcinoma
9. EP176/#1052 Global assessment of BRCA1/2 genetic testing guidelines: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer
10. EP101/#503 Relevance of genomic instability score, tumor mutational burden, and tumor infiltrating lymphocytes as biomarkers in uterine serous carcinoma
11. Systematic mapping review of guidelines forBRCA1/2genetic testing globally: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer
12. Adherence to EndoPredict test scores for extended endocrine therapy management in the prospective EndoPredict Extended Endocrine Trial (EXET).
13. Pancreatic Ductal Carcinoma Risk Associated With Hereditary Cancer-Risk Genes
14. List of Contributors
15. Genetic Counseling: The Role of Genetic Counselors on Healthcare Provider and Endocrinology Teams
16. Computerized Analysis of Digitized Mammograms of Women with Low Breast Cancer Risk and of BRCA1/BRCA2 Gene-Mutation Carriers
17. Infertility, Treatment of Infertility, and the Risk of Breast Cancer among Women with BRCA1 and BRCA2 Mutations: A Case-Control Study
18. eP054: Real-world clinical characteristics and management of breast cancer in patients with germline pathogenic variants in ATM, CHEK2 and PALB2
19. Systematic mapping review of guidelines for BRCA1/2 genetic testing globally: investigating geographic and regional disparities in health equity for women and families at risk for hereditary ovarian cancer.
20. Translational integrity and continuity: Personalized biomedical data integration
21. NSGC Practice Guideline: Risk Assessment and Genetic Counseling for Hereditary Breast and Ovarian Cancer
22. Comprehensive sequencing of PALB2 in patients with breast cancer suggests PALB2 mutations explain a subset of hereditary breast cancer
23. Development and user insights of a novel real-world treatment registry that combines germline hereditary cancer, tumor mutational landscape, and homologous recombination deficiency data with patient clinical characteristics (2179)
24. The Complexity and Challenges of Genetic Counseling and Testing for Inflammatory Bowel Disease
25. Correlates of Depressive Symptoms Among Women Seeking Cancer Genetic Counseling and Risk Assessment at a High-Risk Cancer Clinic
26. The emerging field of polygenic risk scores and perspective for use in clinical care
27. Risk assessment and genetic counseling for hereditary breast and ovarian cancer syndromes—Practice resource of the National Society of Genetic Counselors
28. Genetic testing in an ethnically diverse cohort of high-risk women
29. Incorporating a Psychological Counselor in a Cancer Risk Assessment Program: Necessity, Acceptability, and Potential Roles
30. Contributors
31. Genetic Counseling
32. Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer
33. No Evidence of Increased Risk of Breast Cancer in Women With Lynch Syndrome Identified by Multigene Panel Testing
34. The emerging field of polygenic risk scores and perspective for use in clinical care
35. Pathogenic Variants in BRIP1, RAD51C, and RAD51D Identified with Multi-Gene Panel Testing for Hereditary Cancers
36. Utilization of Complementary Alternative Medicine, Diet, and Exercise Among Women at High Risk for Developing Breast Cancer
37. Learning of your parentʼs BRCA mutation during adolescence or early adulthood: a study of offspring experiences
38. Should genetic testing for BRCA1/2 be permitted for minors? Opinions of BRCA mutation carriers and their adult offspring
39. Cancer Genetic Testing and Assisted Reproduction
40. Book Review: Cancer Genetics for the Clinician. Edited by Gail L. Shaw. Kluwer Academic/Plenum Publishers, New York, 1999, 204 pp. (hardback)
41. Pretest Prediction of BRCA1 or BRCA2 Mutation by Risk Counselors and the Computer Model BRCAPRO
42. Weighing the Risks: Genetic Counseling for Hereditary Breast and Ovarian Cancer
43. Male breast cancer in Cowden syndrome patients with germline PTEN mutations
44. Weighing the Risks:Genetic Counseling for Hereditary Breast and Ovarian Cancer
45. Chapter 28 - Genetic Counseling: The Role of Genetic Counselors on Healthcare Provider and Endocrinology Teams
46. Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer
47. Ancestry-based differences in hereditary cancer genetic testing.
48. Fundamentals of Genetics and Genomics in Oncology Nursing Practice and Navigation.
49. Breast and Ovarian Cancer, Part 2: Counseling Patients About Risk
50. Breast and Ovarian Cancer, Part 1: What You Need to Know About Inherited Risks
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